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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80154Generated: October 26, 2026

Methanol → 2-Fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehyde O-methyl-oxime

https://huagongshe.com/reaction/80154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantO-MethylhydroxylamineHCID 4113—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehydeHCID 59636164—
SolventChloroformHCID 6212—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehyde O-methyl-oximeHCID 866494009.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

O-Methyl-hydroxylamine (84 mg, 1.003 mmol) and K2CO3 (207 mg, 1.5 mmol) were added to a solution of 2-fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehyde-(I-121a: 300 mg, 1.003 mmol) in dimethoxyethane (10 mL). The resulting mixture was heated to 40° C. for 2 hours. The reaction was monitored by TLC (5% MeOH in CHCl3). The reaction mixture was filtered, washed with CHCl3 and the filtrate was concentrated under reduced pressure to afford 30 mg of crude 2-Fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehyde O-methyl-oxime, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045173E1
Source datasetuspto-grants-2014_09
ORD IDord-faec1e1876794e68b942d7f8dbe08414
Source noteuspto-grants-2014_09